The following data is part of a premarket notification filed by Onux Medical, Inc. with the FDA for Non-bioabsorbable Staple.
Device ID | K023372 |
510k Number | K023372 |
Device Name: | NON-BIOABSORBABLE STAPLE |
Classification | Suture, Nonabsorbable, Nitinol |
Applicant | ONUX MEDICAL, INC. 5 MERRILL DR. Hampton, NH 03842 |
Contact | Ruthann Depietro |
Correspondent | Ruthann Depietro ONUX MEDICAL, INC. 5 MERRILL DR. Hampton, NH 03842 |
Product Code | NJU |
CFR Regulation Number | 878.4495 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-10-08 |
Decision Date | 2002-12-27 |
Summary: | summary |